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TANDEM-E HCG CALIBRATION VERIFICATION CONTROL SET

Page Type
Cleared 510(K)
510(k) Number
K920556
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1992
Days to Decision
162 days
Submission Type
Summary

TANDEM-E HCG CALIBRATION VERIFICATION CONTROL SET

Page Type
Cleared 510(K)
510(k) Number
K920556
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1992
Days to Decision
162 days
Submission Type
Summary